Active Ingredients
Menthol 14.5%
Methyl Salicylate 30%
Eagle Oil
FDA Label NDC 43405-005
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Borden Company (private) Limited for the product Eagle (NDC 43405-005). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredients, purpose, uses, warning, do not use, when using this product, stop use and ask a doctor if, keep this drug out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Topical Analgesic
Topical Analgesic
Uses
temporarily relieves the minor aches and pains of muscle and joint associated with : ■ simple backache ■ strains ■ bruises ■ sprains
Warning
For external use only
Do Not Use
■ on woulds or damaged skin ■ with a heating pad
When Using This Product
■ avoid contact with eyes or mucous membranes
■ do not bandage tightly
Stop Use And Ask A Doctor If
■ condition worsens or symptoms persist for more than 7 days ■ symptoms clear up and occur again within a few days ■ excessive skin irritation occurs
Keep This Drug Out Of Reach Of Children
To avoid accidental poisoning, if swallowed, get medical help or contact a Poison Control Center right away.
Directions
■ Use only as directed ■ adults and children 2 years and older: apply to affected area not more than 3 to 4 time daily. ■ children under 2 years of age: ask a doctor
Inactive Ingredients
D&C Green No. 6, D&C Yellow No. 11, ethyl alcohol, mineral oil, rose oil
Question?
1-800-777-6717 or 1-800-645-0789
Package Label
Package Label (Eglemdctedoilrllon)
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